| Transcript Accession | SNP Location | SNP Type | Codon Change | Amino Acid Change | Protein ID |
|---|---|---|---|---|---|
| NM_001282848.1 | 1366 | Missense Mutation | ATT,GTT | I73V | NP_001269777.1 |
| NM_001282849.1 | 1366 | Intron | NP_001269778.1 | ||
| NM_004683.5 | 1366 | Missense Mutation | ATT,GTT | I126V | NP_004674.1 |
| NM_152869.3 | 1366 | Missense Mutation | ATT,GTT | I126V | NP_690608.1 |
| XM_006724567.2 | 1366 | Intron | XP_006724630.1 | ||
| XM_006724568.2 | 1366 | Intron | XP_006724631.1 | ||
| XM_017029954.1 | 1366 | Intron | XP_016885443.1 |